Regulation of ciliary trafficking of polycystin-2 and the pathogenesis of autosomal dominant polycystic kidney disease

Autosomal dominant human hereditary disorder characteristi polycystic kidney disease (ADPKD) is one of the most common c of develop cumulated evidence has suggested that primary cili ment of bilateral multiple fluid-filled kidney cysts. Acum of renal epithelial cell plays a key role in cystogenesis....

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Veröffentlicht in:Zhong nan da xue xue bao. Journal of Central South University. Yi xue ban 2010-02, Vol.35 (2), p.93-99
Hauptverfasser: Cai, Yiqiang, Tang, Zhangui
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container_title Zhong nan da xue xue bao. Journal of Central South University. Yi xue ban
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creator Cai, Yiqiang
Tang, Zhangui
description Autosomal dominant human hereditary disorder characteristi polycystic kidney disease (ADPKD) is one of the most common c of develop cumulated evidence has suggested that primary cili ment of bilateral multiple fluid-filled kidney cysts. Acum of renal epithelial cell plays a key role in cystogenesis. In this article we will give an overview on the basic information about polycystic kidney disease (PKD) and summarize the recent progresses in studies of regulation of polycystin-1 and -2 trafficking to cilia. We will also discuss the possible role of trafficking defects of polycystins on the pathogenesis of ADPKD.
doi_str_mv 10.3969/j.issn.1672-7347.2010.02.001
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issn 1672-7347
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subjects Animals
Cilia - metabolism
Epithelial Cells - metabolism
Humans
Kidney - metabolism
Kidney - pathology
Polycystic Kidney, Autosomal Dominant - etiology
Polycystic Kidney, Autosomal Dominant - genetics
Polycystic Kidney, Autosomal Dominant - metabolism
Protein Transport
Receptors, Cell Surface - genetics
Receptors, Cell Surface - metabolism
Receptors, Cell Surface - physiology
TRPP Cation Channels - genetics
TRPP Cation Channels - metabolism
TRPP Cation Channels - physiology
临床分析
多囊肾
患者
肾衰竭
title Regulation of ciliary trafficking of polycystin-2 and the pathogenesis of autosomal dominant polycystic kidney disease
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